Modulation of MicroRNAs by Euphorbia Microsciadia Boiss in MDA-MB-231 Cell Line: New Possibilities in Breast Cancer Therapy

被引:5
作者
Mahmoudian-Sani, Mohammad-Reza [1 ]
Asadi-Samani, Majid [2 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Thalassemia & Hemoglobinopathy Res Ctr, Hlth Res Inst, Ahvaz, Iran
[2] Shahrekord Univ Med Sci, Cellular & Mol Res Ctr, Basic Hlth Sci Inst, Shahrekord, Iran
关键词
Apoptosis; breast cancer; cell cycle; euphorbia; microRNA; miR-34a; tumor suppressor; MEDICINAL-PLANTS; INDUCED APOPTOSIS; PROLIFERATION; SUPPRESSES; TARGETS; CYCLE; EXPRESSION; MIGRATION; INVASION; THERAPEUTICS;
D O I
10.2174/1574892815666200630102944
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A large number of Euphorbia species have been evaluated for anticancer effects; however, their anticancer mechanisms have not been established up to now. Objective: The present study aimed to evaluate the effects of Euphorbia microsciadia (E. microsciadia) Boiss on the modulation of micro (mi) RNAs in MDA-MB-231 cell line. Methods: As the first step, the inhibitory concentration of hydroalcoholic extract of E. microsciadia on MDA-MB-231 cells was examined using the MTT assay, bypassing 24 and 48h from seeding. The real-time quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR) was also utilized to determine Let-7, miR-15, miR-16, miR-29, miR-151, miR-155, miR-21, miR-146b, miR-181b, miR-221, miR-222, miR-21, and miR-146b expressions in MDA-MB-231 cells, by passing 24 and 48h from treating with the extract of E. microsciadia. Results: The results reveal the cytotoxic effects of E. microsciadia on MDA-MB-231 cell line in a dose-dependent manner. The half maximal Inhibitory Concentrations (IC50) were also equal to 275 and 240 mu g/ml for E. microsciadia, by passing 24 and 48h from the treatment, respectively. Furthermore, it was confirmed that, E. microsciadia had augmented the expression levels of Let-7, miR-15, miR-16, miR-29, and miR-34a, which lead to an increase in apoptosis. Conclusion: E. microsciadia could modulate some miRNAs involved in cell cycle arrest and apoptosis in MDA-MB-231 cell line. Accordingly, targeting miRNAs by E. microsciadia can open some newer avenues for breast cancer therapy.
引用
收藏
页码:174 / 184
页数:11
相关论文
共 84 条
[1]   Contemporary Formulations for Drug Delivery of Anticancer Bioactive Compounds [J].
Ackova, Darinka G. ;
Smilkov, Katarina ;
Bosnakovski, Darko .
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY, 2019, 14 (01) :19-31
[2]   miR-34: from bench to bedside [J].
Agostini, Massimiliano ;
Knight, Richard A. .
ONCOTARGET, 2014, 5 (04) :872-881
[3]   Recent Patents on Anti-Telomerase Cancer Therapy [J].
Agrawal, Apurva ;
Dang, Shweta ;
Gabrani, Reema .
RECENT PATENTS ON ANTI-CANCER DRUG DISCOVERY, 2012, 7 (01) :102-117
[4]   Modification of miRNA Expression through plant extracts and compounds against breast cancer: Mechanism and translational significance [J].
Ahmed, Fayyaz ;
Ijaz, Bushra ;
Ahmad, Zarnab ;
Farooq, Nadia ;
Sarwar, Muhammad Bilal ;
Husnain, Tayyab .
PHYTOMEDICINE, 2020, 68
[5]   Phytochemical Properties and Antibacterial Effects of Salvia multicaulis Vahl., Euphorbia microsciadia Boiss., and Reseda lutea on Staphylococcus aureus and Acinetobacter baumanii [J].
Asadi-Samani, Majid ;
Khaledi, Mansoor ;
Khaledi, Fatemeh ;
Samarghandian, Saeed ;
Gholipour, Abolfazl .
JUNDISHAPUR JOURNAL OF NATURAL PHARMACEUTICAL PRODUCTS, 2019, 14 (03)
[6]  
Asadi-Samani M, 2019, J PHARM PHARMACOGN R, V7, P213
[7]   The effect of Euphorbia szovitsii Fisch. & CAMey extract on the viability and the proliferation of MDA-MB-231 cell line [J].
Asadi-Samani, Majid ;
Rafieian-Kopaei, Mahmoud ;
Lorigooini, Zahra ;
Shirzad, Hedayatollah .
BIOSCIENCE REPORTS, 2019, 39
[8]   A screening of growth inhibitory activity of Iranian medicinal plants on prostate cancer cell lines [J].
Asadi-Samani, Majid ;
Rafieian-Kopaei, Mahmoud ;
Lorigooini, Zahra ;
Shirzad, Hedayatollah .
BIOMEDICINE-TAIWAN, 2018, 8 (02) :16-21
[9]   Direct Serum Assay for MicroRNA-21 Concentrations in Early and Advanced Breast Cancer [J].
Asaga, Sota ;
Kuo, Christine ;
Nguyen, Tung ;
Terpenning, Marilou ;
Giuliano, Armando E. ;
Hoon, Dave S. B. .
CLINICAL CHEMISTRY, 2011, 57 (01) :84-91
[10]  
Ayatollahi AM, 2010, IRAN J PHARM RES, V9, P429